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483
•Curonix LLC•June 24, 2022

Curonix LLC – FDA 483, Jun 24, 2022

Record Details

Stimwave Technologies, Incorporated, a medical device manufacturer in Pompano Beach, FL, was cited for three significant quality system deficiencies during an FDA inspection. The observations included inadequate corrective and preventive action procedures, particularly concerning a patient shock complaint, and issues with process control for product release. Additionally, the firm failed to adequately establish requirements for supplier evaluation.

Company
Curonix LLC
Inspection date
June 24, 2022
Product type
device
Office
Office of Medical Device and Radiological Health Division II
People
  • Ebony D. Sanon
  • Stanley B. Eugene (investigator)
View Company Profile

ID · dc6449e0-b46e-4e76-9814-b4a8eadfc16e

Other documents for Curonix LLC
  • 483 - 2023-11-08November 8, 2023
  • 483 - 2019-02-15February 15, 2019

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